AU2670295A - Process for the preparation of trihydrated cefixime - Google Patents

Process for the preparation of trihydrated cefixime

Info

Publication number
AU2670295A
AU2670295A AU26702/95A AU2670295A AU2670295A AU 2670295 A AU2670295 A AU 2670295A AU 26702/95 A AU26702/95 A AU 26702/95A AU 2670295 A AU2670295 A AU 2670295A AU 2670295 A AU2670295 A AU 2670295A
Authority
AU
Australia
Prior art keywords
tert
trihydrated
cefixime
preparation
cepheme
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
AU26702/95A
Inventor
Carlos Picornell Dardes
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Marcham Trading & Investment Ltd
Original Assignee
Marcham Trading & Investment L
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Marcham Trading & Investment L filed Critical Marcham Trading & Investment L
Publication of AU2670295A publication Critical patent/AU2670295A/en
Abandoned legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D501/00—Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • C07D501/02—Preparation
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D501/00—Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D501/00—Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • C07D501/14—Compounds having a nitrogen atom directly attached in position 7
    • C07D501/16—Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
    • C07D501/20—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
    • C07D501/22—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids with radicals containing only hydrogen and carbon atoms, attached in position 3

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Cephalosporin Compounds (AREA)

Abstract

The invention relates to a process for the preparation of trihydrated cefixime by reacting a functional derivative of N-protected (Z)-2-(2-aminothiazol-4-yl)-2-(tert-butoxycarbonylmethoxyimino)acetic acid with 7-amino-3-vinyl-3-cepheme-4-carboxylate of tert-butyl, or one of the salts thereof and, after removal of the protection group from the product thus obtained, by treating the product of the reaction with aluminium trichloride and anisole. This new process is carried out by using the new intermediate 7 beta -[(Z)-2-(2-aminothiazol-4-yl)-2-(tert-butoxycarbonylmethoxyimino)acetamido]-3-vinyl-3-cepheme-4-carboxylate of tert-butyl, optionally N-protected on the thiazolic amine.
AU26702/95A 1994-06-03 1995-05-10 Process for the preparation of trihydrated cefixime Abandoned AU2670295A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
CH01751/94A CH688319A5 (en) 1994-06-03 1994-06-03 Process for the preparation of cefixime trihydrate.
CH1751/94 1994-06-03
PCT/EP1995/001759 WO1995033753A1 (en) 1994-06-03 1995-05-10 Process for the preparation of trihydrated cefixime

Publications (1)

Publication Number Publication Date
AU2670295A true AU2670295A (en) 1996-01-04

Family

ID=4217712

Family Applications (1)

Application Number Title Priority Date Filing Date
AU26702/95A Abandoned AU2670295A (en) 1994-06-03 1995-05-10 Process for the preparation of trihydrated cefixime

Country Status (9)

Country Link
EP (1) EP0763043B1 (en)
KR (1) KR100223384B1 (en)
AT (1) ATE171454T1 (en)
AU (1) AU2670295A (en)
CH (1) CH688319A5 (en)
DE (1) DE69504971T2 (en)
ES (1) ES2120911B1 (en)
PE (1) PE13296A1 (en)
WO (1) WO1995033753A1 (en)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6204261B1 (en) 1995-12-20 2001-03-20 Vertex Pharmaceuticals Incorporated Inhibitors of interleukin-1β Converting enzyme inhibitors
US6420522B1 (en) 1995-06-05 2002-07-16 Vertex Pharmaceuticals Incorporated Inhibitors of interleukin-1β converting enzyme
AT404251B (en) * 1996-08-14 1998-10-27 Biochemie Gmbh NEW CRYSTALLINE SALT FROM CEFIXIM
PT102061B (en) * 1997-10-08 2000-06-30 J K Ind Ltd PROCESS OF PREPARATION OF AN ECHALOSPORIN ANTIBIOTIC ACID GENERALLY ACTIVE-CEFIXIME
US20040166434A1 (en) 2003-02-21 2004-08-26 Dammel Ralph R. Photoresist composition for deep ultraviolet lithography
ATE423123T1 (en) 2004-12-21 2009-03-15 Lupin Ltd METHOD FOR PRODUCING CEFIXIM
EP1863822B1 (en) 2005-03-29 2009-10-14 Hetero Drugs Limited An improved process for the preparation of cefixime
CN1312158C (en) * 2005-05-20 2007-04-25 天津市医药集团技术发展有限公司 Method for preparing cefixime
WO2016142902A1 (en) * 2015-03-11 2016-09-15 Lupin Limited Cefixime with reduced surface area and high stability
CN111039958B (en) * 2017-05-31 2022-05-20 郑州大学第一附属医院 Preparation method of cefdinir
JP2023011144A (en) 2021-07-12 2023-01-24 ウシオ電機株式会社 Light source device, lighting circuit for dielectric barrier discharge lamp, and lighting method for dielectric barrier discharge lamp
CN113968874B (en) * 2021-10-29 2023-01-31 国药集团威奇达药业有限公司 Refining method of cefixime

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4409214A (en) * 1979-11-19 1983-10-11 Fujisawa Pharmaceutical, Co., Ltd. 7-Acylamino-3-vinylcephalosporanic acid derivatives and processes for the preparation thereof

Also Published As

Publication number Publication date
KR100223384B1 (en) 1999-10-15
ES2120911B1 (en) 1999-07-01
DE69504971D1 (en) 1998-10-29
EP0763043A1 (en) 1997-03-19
ES2120911A1 (en) 1998-11-01
EP0763043B1 (en) 1998-09-23
ATE171454T1 (en) 1998-10-15
KR970703348A (en) 1997-07-03
CH688319A5 (en) 1997-07-31
WO1995033753A1 (en) 1995-12-14
PE13296A1 (en) 1996-05-10
DE69504971T2 (en) 1999-05-20

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